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Phase 1a First-in-Human Study of Safety and Tolerability of ASV AGEN2017 With QS-21 Stimulon Adjuvant as a Single Agent in Subjects With Solid Tumor at Risk of Relapse Undergoing Observation as SOC Following Complete Surgical Resection

Trial Profile

Phase 1a First-in-Human Study of Safety and Tolerability of ASV AGEN2017 With QS-21 Stimulon Adjuvant as a Single Agent in Subjects With Solid Tumor at Risk of Relapse Undergoing Observation as SOC Following Complete Surgical Resection

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 01 Aug 2019

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At a glance

  • Drugs AutoSynVax (Primary) ; QS 21 (Primary)
  • Indications Bladder cancer; Breast cancer; Cervical cancer; Colorectal cancer; Head and neck cancer; Malignant melanoma; Non-small cell lung cancer; Renal cancer; Soft tissue sarcoma; Solid tumours
  • Focus Adverse reactions; First in man
  • Sponsors Agenus
  • Most Recent Events

    • 18 May 2019 Planned End Date changed from 1 Jun 2020 to 1 Dec 2020.
    • 18 May 2019 Planned primary completion date changed from 1 Jan 2020 to 1 Aug 2020.
    • 31 Oct 2018 Status changed from not yet recruiting to recruiting.
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